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Lucy Zheng

Explore the profile of Lucy Zheng including associated specialties, affiliations and a list of published articles. Areas
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Articles 8
Citations 57
Followers 0
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Recent Articles
1.
Merdler I, Case B, Collins E, Rahman S, Reddy P, Bhogal S, et al.
Am J Cardiol . 2023 Sep; 205:454-456. PMID: 37666018
No abstract available.
2.
Zheng L, Zheng X
Ann Blood . 2023 May; 8. PMID: 37200543
No abstract available.
3.
Zheng L, Hill J, Zheng L, Rumi M, Zheng X
J Clin Transl Pathol . 2022 Oct; 2(3):108-115. PMID: 36276172
Background And Objectives: Genotyping is an important tool for studying gene functions in animals or detecting genetic variants in humans. Various methods using low to high concentrations of agarose or...
4.
Neelon M, Price N, Srivastava D, Zheng L, Trzesniewski K
J Nutr Educ Behav . 2022 Aug; 54(10):902-907. PMID: 35970730
Objective: Examine the association between educational attainment and improvement in food practice outcomes of the California Expanded Food and Nutrition Education Program (EFNEP) participants. Design: Secondary data analysis. Participants: A...
5.
Ramaswamy K, Madariaga H, Zheng L, Thomas B, Lerma E
Dis Mon . 2022 Feb; 68(12):101330. PMID: 35221018
No abstract available.
6.
Fusco A, McCall A, Dhindsa J, Zheng L, Bailey A, Kahn A, et al.
Int J Mol Sci . 2020 Mar; 21(6). PMID: 32214050
Pompe disease is a glycogen storage disease caused by a deficiency in acid α-glucosidase (GAA), a hydrolase necessary for the degradation of lysosomal glycogen. This deficiency in GAA results in...
7.
Chatterjee S, Zheng L, Ma S, Bedja D, Bandaru V, Kim G, et al.
Biochem Biophys Res Commun . 2020 Feb; 525(2):455-461. PMID: 32107002
Metabolic syndrome is defined by hyperlipidemia and cardiovascular complications. We have examined whether inhibition of glycosphingolipid synthesis can interfere with metabolic syndrome in a male mouse model of type II...
8.
Staley E, Cao W, Pham H, Kim C, Kocher N, Zheng L, et al.
Haematologica . 2018 Sep; 104(1):166-175. PMID: 30171022
Immune-mediated thrombotic thrombocytopenic purpura is characterized by severe thrombocytopenia and microangiopathic hemolytic anemia. It is primarily caused by immunoglobin G type autoantibodies against ADAMTS13, a plasma metalloprotease that cleaves von...